Canonical Allele Identifier: CA1880332739

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540644C= , CM000671.2:g.128540644C=	GRCh38
NC_000009.11:g.131302923C= , CM000671.1:g.131302923C=	GRCh37
NC_000009.10:g.130342744C=	NCBI36
NG_012073.1:g.40953C= , LRG_484:g.40953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1099+306C=	ENSP00000507095.1:n.*1099+306C=
ENST00000683288.1:c.*2027+306C=	ENSP00000507477.1:n.*2027+306C=
ENST00000683748.1:c.2055+306C=	ENSP00000507377.1:n.2055+306C=
ENST00000683905.1:c.*704+306C=	ENSP00000506960.1:n.*704+306C=
ENST00000684139.1:c.1563+306C=	ENSP00000507295.1:n.1563+306C=
ENST00000684210.1:n.1741+306C=
ENST00000684314.1:c.1923+306C=	ENSP00000507700.1:n.1923+306C=
ENST00000684331.1:c.*291C=	ENSP00000507431.1:n.*291C=
ENST00000684463.1:n.666+306C=
ENST00000684646.1:c.1815+306C=	ENSP00000507723.1:n.1815+306C=
ENST00000309971.9:c.2028+306C= MANE Select	ENSP00000308622.5:n.2028+306C=
ENST00000309971.8:c.2028+306C=	ENSP00000308622.4:n.2028+306C=
NM_001003722.1:c.2028+306C= , LRG_484t1:c.2028+306C=	NP_001003722.1:n.2028+306C=
XM_006717059.2:c.2064+306C=	XP_006717122.1:n.2064+306C=
XM_006717060.2:c.2037+306C=	XP_006717123.1:n.2037+306C=
XM_011518549.1:c.2064+306C=	XP_011516851.1:n.2064+306C=
XM_011518550.1:c.2064+306C=	XP_011516852.1:n.2064+306C=
XM_011518551.1:c.2055+306C=	XP_011516853.1:n.2055+306C=
XM_011518552.1:c.1305+306C=	XP_011516854.1:n.1305+306C=
XR_242681.3:n.100+2735G=
XR_428600.2:n.124+326G=
XM_006717059.3:c.2064+306C=	XP_006717122.1:n.2064+306C=
XM_006717060.3:c.2037+306C=	XP_006717123.1:n.2037+306C=
XM_011518551.2:c.2055+306C=	XP_011516853.1:n.2055+306C=
XM_024447519.1:c.2037+306C=	XP_024303287.1:n.2037+306C=
XR_428600.3:n.126+326G=
NM_001003722.2:c.2028+306C= MANE Select	NP_001003722.1:n.2028+306C=